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Volumn 3, Issue 21, 2013, Pages 7751-7757

An exclusive approach to 3,4-disubstituted cyclopentenes and alkylidene cyclopentenes via the palladium catalyzed ring opening of azabicyclic olefins with aryl halides

Author keywords

[No Author keywords available]

Indexed keywords

ARYL HALIDES; BICYCLIC HYDRAZINE; CYCLOPENTENES; FUNCTIONALIZATIONS; MULTIPLE POINTS; PALLADIUM CATALYSIS; PALLADIUM-CATALYZED; STEREO-SELECTIVE;

EID: 84877692043     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c3ra41504j     Document Type: Article
Times cited : (15)

References (40)
  • 35
    • 78650326847 scopus 로고    scopus 로고
    • This reduction presumably proceeds via oxidative addition of the R-C-H bond of triethylamine to Pd, followed by fragmentation of the resulting species. See also
    • B. A. Bhanu Prasad A. E. Buechele S. R. Gilbertson Org. Lett. 2010 12 5422
    • (2010) Org. Lett. , vol.12 , pp. 5422
    • Bhanu Prasad, B.A.1    Buechele, A.E.2    Gilbertson, S.R.3
  • 38
    • 0000070366 scopus 로고
    • In our initial report, 9 toluene was used as the solvent and the maximum yield was only 60%
    • S.-I. Murahashi T. Watanabe J. Am. Chem. Soc. 1979 101 7429
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 7429
    • Murahashi, S.-I.1    Watanabe, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.